Evidence map›Paper›PMID 37611321›Full record

ArticleAdvanced healthcare materials2023

Photopolymerizable Hydrogel for Enhanced Intramyocardial Vascular Progenitor Cell Delivery and Post-Myocardial Infarction Healing.

Xuechong Hong, Allen Chilun Luo, Ilias Doulamis, Nicholas Oh, Gwang-Bum Im, Chun-Yen Lin, Pedro J Del Nido, Ruei-Zeng Lin, Juan M Melero-Martin

Open access · bronzeAbstract read
In one paragraph

Article in Advanced healthcare materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Xuechong HongDepartment of Cardiac Surgery, Boston Children's Hospital, Boston, MA, 02115, USA.
Allen Chilun LuoDepartment of Cardiac Surgery, Boston Children's Hospital, Boston, MA, 02115, USA.
Ilias DoulamisDepartment of Cardiac Surgery, Boston Children's Hospital, Boston, MA, 02115, USA.
Nicholas OhDepartment of Cardiac Surgery, Boston Children's Hospital, Boston, MA, 02115, USA.
Gwang-Bum ImDepartment of Cardiac Surgery, Boston Children's Hospital, Boston, MA, 02115, USA.
Chun-Yen LinDepartment of Lymphoma and Myeloma, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, 77030, USA.
Pedro J Del NidoDepartment of Cardiac Surgery, Boston Children's Hospital, Boston, MA, 02115, USA.
Ruei-Zeng LinDepartment of Cardiac Surgery, Boston Children's Hospital, Boston, MA, 02115, USA.
Juan M Melero-MartinDepartment of Cardiac Surgery, Boston Children's Hospital, Boston, MA, 02115, USA.ORCID 0000-0002-4689-8149
Boston Children's Hospital · USThe University of Texas MD Anderson Cancer Center · US

Funding

Vascular networks genetically engineered for protein drug deliveryR01HL128452 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI MELERO-MARTIN, JUAN M, WANG, BO · 2015 to 2024
$4.8M
Enhancing endothelial cell engraftment via transplantation of exogenous mitochondriaR01HL152133 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI Juan M Melero-Martin · 2021 to 2026
$3.1M
Human endothelial cell regulation of ossificationR01AR080086 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI Juan M Melero-Martin · 2022 to 2026
$2.1M
NHLBI NIH HHS R01 HL128452NHLBI NIH HHS R01 HL152133NIAMS NIH HHS R01 AR080086NIH HHS R01AR080086 to J.M.M.-MNIH HHS R01HL128452NIH HHS R01HL152133
6 · The paper itself

Abstract

Cell transplantation success for myocardial infarction (MI) treatment is often hindered by low engraftment due to washout effects during myocardial contraction. A clinically viable biomaterial that enhances cell retention can optimize intramyocardial cell delivery. In this study, a therapeutic cell delivery method is developed for MI treatment utilizing a photocrosslinkable gelatin methacryloyl (GelMA) hydrogel. Human vascular progenitor cells, capable of forming functional vasculatures upon transplantation, are combined with an in situ photopolymerization approach and injected into the infarcted zones of mouse hearts. This strategy substantially improves acute cell retention and promotes long-term post-MI cardiac healing, including stabilized cardiac functions, preserved viable myocardium, and reduced cardiac fibrosis. Additionally, engrafted vascular cells polarize recruited bone marrow-derived neutrophils toward a non-inflammatory phenotype via transforming growth factor beta (TGFβ) signaling, fostering a pro-regenerative microenvironment. Neutrophil depletion negates the therapeutic benefits generated by cell delivery in ischemic hearts, highlighting the essential role of non-inflammatory, pro-regenerative neutrophils in cardiac remodeling. In conclusion, this GelMA hydrogel-based intramyocardial vascular cell delivery approach holds promise for enhancing the treatment of acute myocardial infarction.

Indexed as

HydrogelsMyocardial InfarctionAnimalsHumansMiceMyocardiumStem CellsHydrogelscell deliverygelatin methacryloylmyocardial infarctionpro-regenerative neutrophil

Identifiers

PMID37611321
PMCPMC10840685
OpenAlexW4386090047

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.